The Gene for Human Liver Arginase (ARG1) is Assigned to Chromosome Band 6q23

Overview

Journal Am J Hum Genet

Publisher Cell Press

Specialty Genetics

Date 1986 Aug 1

PMID 3752085

Citations 29

Authors

R S Sparkes

G J Dizikes

I Klisak

W W Grody

T Mohandas

C Heinzmann

S Zollman

A J Lusis

S D Cederbaum

Affiliations

Soon will be listed here.

Abstract

The human liver arginase gene, whose deficiency is responsible for argininemia (McKusick no. 20780), has been assigned to 6q23 through a combination of somatic cell hybrid analysis and in situ hybridization using a 1,550-base pair (bp) human DNA probe for this gene.

Citing Articles

ACMG/AMP variant classification framework in arginase 1 deficiency: Implications for birth prevalence estimates and diagnostics.

Cameron J, Osundiji M, Olson R, Olarewaju B, Schulze A Genet Med Open. 2024; 2:101815.

PMID: 39669610 PMC: 11613747. DOI: 10.1016/j.gimo.2024.101815.

Arginase: Biological and Therapeutic Implications in Diabetes Mellitus and Its Complications.

Ren Y, Li Z, Li W, Fan X, Han F, Huang Y Oxid Med Cell Longev. 2022; 2022:2419412.

PMID: 36338341 PMC: 9629921. DOI: 10.1155/2022/2419412.

Arginase Gene Polymorphism Increases Risk of Diabetic Retinopathy in Type 2 Diabetes Mellitus Patients.

Buraczynska M, Zakrocka I J Clin Med. 2021; 10(22).

PMID: 34830689 PMC: 8620112. DOI: 10.3390/jcm10225407.

Novel ARG1 variants identified in a patient with arginase 1 deficiency.

Yokoi K, Nakajima Y, Yasui T, Yoshino M, Yoshikawa T, Kurahashi H Hum Genome Var. 2021; 8(1):8.

PMID: 33542202 PMC: 7862390. DOI: 10.1038/s41439-021-00139-9.

Association analysis between ARG1 gene polymorphisms and idiopathic dilated cardiomyopathy.

Shah S, Akram S, Iqbal T, Nawaz S, Rafiq M, Hussain S Medicine (Baltimore). 2019; 98(47):e17694.

PMID: 31764771 PMC: 6882636. DOI: 10.1097/MD.0000000000017694.

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